Clinical Research Coordinator

Job overview

The Clinical Research Coordinator role is onsite in Las Vegas, NV, with a 40-hour schedule. Compensation is not specified. System One provides outsourced services and workforce solutions to help clients complete work efficiently without compromising quality. The coordinator supports clinical research protocols under the supervision of the principal investigator and senior research staff. The role helps ensure participant visits, study documentation, data collection, and protocol-related reporting are completed in accordance with research and regulatory standards.

What you'll do

• Assist with coordination and execution of clinical research protocols
• conduct participant screening visits
• assist with informed consent and enrollment
• schedule study visits, procedures, and follow-ups
• collect and maintain research data and source documentation
• educate participants and answer questions
• report adverse events and protocol deviations
• follow SOPs and GCP guidelines
• draw, process, and ship specimens if qualified
• maintain study records
• support study operations and problem resolution.

What we're looking for

Skills & competencies

clinical research coordinator

clinical research

clinical trials

participant screening

informed consent

gcp

hipaa

las vegas nv

system one

40 hours

onsite

Work arrangement

• Weekend coverage required

Benefits & perks

• Eligible employees may have medical, dental, vision, spending accounts, life insurance, voluntary plans, and 401(k) benefits.

Why this role

High school diploma or equivalent required; an associate’s degree or higher in a health-related field is preferred. Medical terminology and patient care experience are required. Specimen handling is conditional on qualification; several certifications and research skills are preferred.

About the employer

The Davey Tree Expert Company is hiring for this role. Industry: Offices of Physicians (except Mental Health Specialists). Sector: 62.